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- W2414909421 abstract "A formal synthesis of (-)-schulzeine B, a marine natural alkaloid possessing potent antidiabetic activity, has been achieved. A benzo[a]quinolizidin-4-one is a common skeleton of schulzeines (A-C). (-)-Schulzeine B possesses an (S)-stereogenic center at the C-3 carbon. The chiral (3S,11bS)-3-amino-9,11-dimethoxybenzo[a]quinolizidin-4-one has been prepared efficiently from (2-bromo-3,5-dihydroxyphenyl)acetonitrile in 17 steps including (i) a dehydrative intramolecular amination catalyzed by HClO4 and (ii) a proline or boric acid catalyzed transcycloamidation reaction for the construction of the δ-lactam ring." @default.
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- W2414909421 date "2015-07-28" @default.
- W2414909421 modified "2023-10-09" @default.
- W2414909421 title "Synthesis of the Core Tricyclic Ring Domain of (−)-Schulzeine B" @default.
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- W2414909421 doi "https://doi.org/10.1021/acs.joc.5b01173" @default.
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